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OncoMatch/Clinical Trials/NCT05417165

Anti-pneumococcal Vaccine Strategy in Patients With Chronic Lymphocytic Leukemia

Is NCT05417165 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Pneumococcal 20-valent Conjugate Vaccine and Pneumococcal Polyvalent Vaccine for chronic lymphocytic leukemia.

Phase 2RecruitingSeema BhatNCT05417165Data as of May 2026

Treatment: Pneumococcal 20-valent Conjugate Vaccine · Pneumococcal Polyvalent VaccineThis phase II trial compares the effect of initial vaccination (PCV20 followed by PSV23) with yearly vaccinations of PSV23 to the standard 5 year vaccination in patients with chronic lymphocytic leukemia. At present chronic lymphocytic leukemia patients are poorly protected by anti-pneumococcal vaccination. Current vaccination schedule for chronic lymphocytic leukemia patients is based on general recommendations in immunocompromised patients (initial vaccination with PCV13 followed by one dose of PSV23 after an interval of two months, followed by revaccination at 5 years). Giving patients frequent immunization as compared to 5 year immunization may result in higher protective titers in patients.

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Extracted eligibility criteria

Cancer type

Chronic Lymphocytic Leukemia

Non-Hodgkin Lymphoma

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: chemotherapy

No prior therapy for CLL/SLL, including chemotherapy and/or radiotherapy is allowed

Cannot have received: radiation therapy

No prior therapy for CLL/SLL, including chemotherapy and/or radiotherapy is allowed

Cannot have received: anti-CD20 monoclonal antibody (rituximab)

having received rituximab within 6 months

Cannot have received: anti-CD20 monoclonal antibody (rituximab)

Exception: for non-hematological indications

received Rituximab or similar anti CD20 monoclonal antibody for non-hematological indications within 6 months

Cannot have received: intravenous immunoglobulin (IVIG)

Received intravenous immunoglobulin (IVIG) within 3 months prior to vaccination

Cannot have received: cellular therapy (CAR-T cells)

Patients who have received cellular therapy (e.g. CAR-T cells) within 12 months prior to vaccination

Cannot have received: stem cell transplant

History of allogenic stem cell transplantation

Cannot have received: pneumococcal vaccine

Patients who have previously received pneumococcal vaccine within the preceding 12 months

Lab requirements

Blood counts

neutropenic (granulocyte [PMN]s < 500 cells/mm^3) or absolute lymphocyte count less than 500 cells/mm^3 excluded

Patients with neutropenic (granulocyte [PMN]s < 500 cells/mm^3) or absolute lymphocyte count less than 500 cells/mm^3

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Ohio State University Comprehensive Cancer Center · Columbus, Ohio

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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